Target Name: HEXA
NCBI ID: G3073
Review Report on HEXA Target / Biomarker Content of Review Report on HEXA Target / Biomarker
HEXA
Other Name(s): Hexosaminidase subunit A | hexosaminidase subunit alpha | beta-N-Acetylhexosaminidase | TSD | Beta-hexosaminidase subunit alpha (isoform 2) | HEXA_HUMAN | Hexosaminidase subunit alpha, transcript variant 2 | hexosaminidase subunit A | HEXA variant 2 | Hexosaminidase A | Beta-N-acetylhexosaminidase subunit alpha | beta-N-acetylhexosaminidase subunit alpha | N-acetyl-beta-glucosaminidase | Beta-hexosaminidase subunit alpha | N-acetyl-beta-glucosaminidase subunit alpha | hexosaminidase A (alpha polypeptide)

HEXA: A Promising Drug Target / Biomarker

Hexa is a protein that is expressed in various tissues of the body, including the brain, heart, and kidneys. Its primary function is to transport and regulate the transport of different molecules across cell membranes. It is a key protein that is involved in many physiological processes in the body, including cell signaling, neurotransmitter transport, and inflammation.

Recent studies have suggested that Hexa may have potential as a drug target or biomarker. This is because the protein is involved in many different processes in the body, and many diseases are caused by problems with the transport of molecules across cell membranes. By targeting Hexa and inhibiting its function, researchers may be able to develop new treatments for a variety of diseases.

Hexa Structure and Function

Hexa is a member of the protein family known as the transmembrane protein (TMP) family. This family of proteins is known for their ability to transport a wide variety of molecules across cell membranes, including ions, nutrients, and toxins. Hexa is characterized by its six transmembrane domains, which are responsible for its unique structure and function.

One of the key features of Hexa is its ability to form a pore in the cell membrane. This pore, called a channels, allows the protein to transport different molecules across the membrane. Hexa is able to form this pore by using a unique protein called HexA, which is located in the cytoplasm.

HexA is a small protein that is composed of 110 amino acids. It has been shown to play a key role in the formation of the channels that allow Hexa to transport molecules across the cell membrane. HexA is able to form these channels by using a unique process called self-assembly, which involves the formation of a protein structure that is too large to fit into the cell membrane.

Drug Targeting

Hexa has been shown to be involved in many different processes in the body, including cell signaling, neurotransmitter transport, and inflammation. This makes it an attractive target for drug development. By inhibiting Hexa function, researchers may be able to develop new treatments for a variety of diseases.

One of the key challenges in developing drugs that target Hexa is its widespread distribution in the body. Because it is expressed in many different tissues and organs, it is difficult to predict where a drug will be most effective. However, researchers are making progress in understanding the molecular mechanisms that Hexa uses to transport molecules across the cell membrane, and are using this information to develop new drugs.

Biomarker

Hexa may also be useful as a biomarker for certain diseases. By measuring the level of Hexa in different tissues or fluids, researchers can monitor the effectiveness of a drug or determine if a patient has a particular disease. For example, Hexa has been used as a biomarker to measure the effectiveness of a drug for treating Alzheimer's disease.

Conclusion

Hexa is a protein that is involved in many different physiological processes in the body. Its unique structure and function make it an attractive target for drug development, and its widespread distribution in the body makes it a valuable biomarker for certain diseases. Further research is needed to fully understand the molecular mechanisms that Hexa uses to transport molecules across the cell membrane, and to develop new treatments for a variety of diseases.

Protein Name: Hexosaminidase Subunit Alpha

Functions: Hydrolyzes the non-reducing end N-acetyl-D-hexosamine and/or sulfated N-acetyl-D-hexosamine of glycoconjugates, such as the oligosaccharide moieties from proteins and neutral glycolipids, or from certain mucopolysaccharides (PubMed:11707436, PubMed:9694901, PubMed:8672428, PubMed:8123671). The isozyme S is as active as the isozyme A on the anionic bis-sulfated glycans, the chondroitin-6-sulfate trisaccharide (C6S-3), and the dermatan sulfate pentasaccharide, and the sulfated glycosphingolipid SM2 (PubMed:11707436). The isozyme B does not hydrolyze each of these substrates, however hydrolyzes efficiently neutral oligosaccharide (PubMed:11707436). Only the isozyme A is responsible for the degradation of GM2 gangliosides in the presence of GM2A (PubMed:9694901, PubMed:8672428, PubMed:8123671)

The "HEXA Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about HEXA comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

More Common Targets

HEXA-AS1 | HEXB | HEXD | HEXIM1 | HEXIM2 | Hexokinase | HEY1 | HEY2 | HEY2-AS1 | HEYL | HFE | HFM1 | HGC6.3 | HGD | HGF | HGFAC | HGH1 | HGS | HGSNAT | HHAT | HHATL | HHEX | HHIP | HHIP-AS1 | HHIPL1 | HHIPL2 | HHLA1 | HHLA2 | HHLA3 | HIBADH | HIBCH | HIC1 | HIC2 | HID1 | HID1-AS1 | HIF1A | HIF1A-AS1 | HIF1A-AS2 | HIF1A-AS3 | HIF1AN | HIF3A | HIGD1A | HIGD1AP1 | HIGD1AP10 | HIGD1B | HIGD1C | HIGD2A | HIGD2B | High affinity cAMP-specif | High Affinity Immunoglobulin Epsilon Fc Receptor | HIKESHI | HILPDA | HILPDA-AS1 | HINFP | HINT1 | HINT1P1 | HINT2 | HINT3 | HIP1 | HIP1R | HIPK1 | HIPK1-AS1 | HIPK2 | HIPK3 | HIPK4 | HIRA | HIRIP3 | HISLA | Histamine Receptor (HR) | Histocompatibility antigen-related | Histone | Histone acetyltransferase (HAT) | Histone deacetylase | Histone H2A | Histone H2B | Histone H3 | Histone Lysine Demethylase | Histone methyltransferase | HIVEP1 | HIVEP2 | HIVEP3 | HJURP | HJV | HK1 | HK2 | HK2P1 | HK3 | HKDC1 | HLA Class II Histocompatibility Antigen DM (HLA-DM) | HLA class II histocompatibility Antigen DO (HLA-DO) | HLA class II histocompatibility antigen DP (HLA-DP) | HLA Class II Histocompatibility Antigen DQ8 | HLA class II histocompatibility antigen DR (HLA-DR) | HLA Class II Histocompatibility Antigen, DQ (HLA-DQ) | HLA class II histocompatibility antigen, DRB1-7 beta chain, transcript variant X1 | HLA complex group 16 (non-protein coding), transcript variant X2 | HLA complex group 8 | HLA-A | HLA-B | HLA-C